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rs796065343

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796065343(C;T)
Make rs796065343(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position36467833
GeneCSF3R
is asnp
is mentioned by
dbSNPrs796065343
ebirs796065343
HLIrs796065343
Exacrs796065343
Varsomers796065343
Maprs796065343
PheGenIrs796065343
hapmaprs796065343
1000 genomesrs796065343
hgdprs796065343
ensemblrs796065343
gopubmedrs796065343
geneviewrs796065343
scholarrs796065343
googlers796065343
pharmgkbrs796065343
gwascentralrs796065343
openSNPrs796065343
23andMers796065343
23andMe allrs796065343
SNP Nexus

SNPshotrs796065343
SNPdbers796065343
MSV3drs796065343
GWAS Ctlgrs796065343
Max Magnitude0
ClinVar
Risk rs796065343(T;T)
Alt rs796065343(T;T)
Reference rs796065343(C;C)
Significance Pathogenic
Disease Early T cell progenitor acute lymphoblastic leukemia
Variation info
Gene CSF3R
CLNDBN Early T cell progenitor acute lymphoblastic leukemia
Reversed 1
HGVS NC_000001.10:g.36933434G>A
CLNSRC
CLNACC RCV000190419.1,